- Teleflex (Morrisville, NC)
- …primary point of contact and coordinator of the global business process for medical device sustaining engineering projects * Generate the R&D department monthly ... the operating procedures and policies of the work unit. ** Principal Responsibilities** * Supervise and mentor a team of...professionals * Experience within a regulated industry, such as medical device or pharmaceutical, is preferred *… more
- Teleflex (Coventry, CT)
- …is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... is preferred or 3+ years of Quality Assurance experience working in the medical device manufacturing environment (a combination of education and experience will… more
- Williams Companies (Tulsa, OK)
- …equipment. + Conducts in-depth power system analyses, including short-circuit, protective device coordination, arc flash hazard, harmonics, voltage drop, load flow, ... Proficient with engineering tools: SKM Power Systems, ETAP, GE Multilin, SEL Relay Software + Knowledge of applicable codes and standards (API, IEEE, NESC, NEC,… more
- J&J Family of Companies (Cincinnati, OH)
- …and written communication skills **Preferred Skills & Experiences:** + Experience within a medical device or other highly regulated industry + Clinical knowledge ... talent to join our MedTech team in Cincinnati, OH as a Senior Principal Engineer, R&D External Innovation! **Position Overview:** The Senior Principal Engineer,… more
- Teleflex (Morrisville, NC)
- …experience in project or program management working in a technical discipline, medical device and/or engineering preferred. * Proficiency with design control ... :12477 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...involved with engineering and cross-functional teams in the hardware, software systems space. This position is part of the… more
- Teleflex (Wyomissing, PA)
- …* Minimum of 3 years of previous experience in related field (eg medical device design and manufacturing, or similar regulated industry, plastic processing, ... of Design for Manufacturability (DFM) principles and basic ergonomic considerations in medical device design. * Understanding of verification and validation… more
- Hologic (Newark, DE)
- …a visionary leader with a passion for ensuring the highest standards of quality in medical device design and development? We are seeking a dynamic **Director of ... in FDA Quality System Regulations, especially Design Control requirements, ISO 13485, and Medical Device Directive. + Familiarity with ISO 14970, IEC 60601, IEC… more
- ConvaTec (Lexington, MA)
- …8-10 years of experience in clinical data management or a similar role in the medical device or clinical research industry. + Proven track record of building and ... **About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:**...Contribute to the development and validation of data management software tools. + Oversee the data analytics for Convatec… more
- University of Rochester (Rochester, NY)
- …+ May conduct telephone interviews to screen potential study candidates. + Reviews medical chart history with Principal Investigator to verify inclusion criteria ... with protocol requirements, such as taking of medications, proper use of device , and/or other interventional activities, to document adverse events and report to… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... to act as implementation subject matter expert for one or more Medical Informatics products. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're… more